NDC 48951-2137-03 - Bryophyllum Avena
This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
- Product NDC
- 48951-2137
- Requested NDC
- 48951-2137-03
- Package NDCs from labels
- 48951-2137-3, 48951-2137-03
- Manufacturer
- Uriel Pharmacy Inc
- Effective date
- 2025-05-28
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Bryophyllum Avena - Uriel Pharmacy Inc | Uriel Pharmacy Inc | 2025-05-28 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 48951-2137-3 | Bryophyllum Avena | 60 mL in 1 BOTTLE, DROPPER | LIQUID | 60 | 5 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 48951-2137 | BRYOPHYLLUM AVENA LIQUID [URIEL PHARMACY INC] | 4 | Current NDC, Legacy NDC, 1 package rows | 20240118_f3d21630-0a99-11df-8a39-0800200c9a66.zip |
DailyMed Socrata Ingredients#
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
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| Sodium Sulfacetamide and Sulfur | SULFACETAMIDE SODIUM, SULFUR | Bryant Ranch Prepack | dafae162-9cae-4ba6-b8af-8c9bbc0f0010 | 2026-06-01 | Warnings | 70FD1KFU70 |
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Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.